Broadwell R D, Cataldo A M
J Comp Neurol. 1984 Dec 1;230(2):231-48. doi: 10.1002/cne.902300208.
The morphology and cytochemistry of the endoplasmic reticulum (ER) in axons and terminals of a number of different types of neurons in brains from mice were investigated ultrastructurally. The neurohypophysis received particular attention because the morphology and enzyme cytochemical activities of many of the preterminal swellings of hypothalamo-neurohypophysial axons are altered by chronic salt-stress. Membrane contrast and enzyme cytochemical staining techniques were employed to characterize the axonal reticulum and to determine if organelles representing the lysosomal system in the axon and the tubular profiles participating in the anterograde axonal transport of native horseradish peroxidase (HRP) are associated with the ER. Potential enzyme cytochemical markers for the axonal ER included glucose-6-phosphatase (G6Pase), thiamine pyrophosphatase, nucleoside diphosphatase, and acid hydroxylase activities. The anterograde transport of HRP was analyzed in undamaged hypothalamo-neurohypophysial neurons and in facial and hypoglossal motoneurons of mice receiving the protein in the lateral cerebral ventricle. The ER pervaded the axon and appeared as parallel, 20-40-nm-wide tubules interconnected by oblique anastomoses. Membrane thickness of the axonal reticulum measured 60-100 A, which is similar to that of the perikaryal ER. Enzyme cytochemical activities associated with the ER or lysosomes were not conspicuous in axons and terminals under normal conditions but became prominent in some axons and preterminal swellings manifesting an autophagic appearance within neurohypophyses from salt-stressed mice. Only G6Pase activity was a marker for the ER in these axons and preterminals. Many ER profiles in non-incubated sections and in G6Pase cytochemical preparations of salt-stressed neurohypophyses were wrapped around or interspersed among secretory granules, multilamellar bodies, and vacuoles that may represent forms of lysosomes involved in autophagy and crinophagy. Acid hydrolase activities were localized within the vacuoles as well as within 80-130-nm-wide, blunt-ended tubules in pituitary stalk axons; similar reactive tubules were confluent with large secondary lysosomes in neurosecretory cell bodies and may be derived from these lysosomes. Morphologically identical tubules transporting HRP in the anterograde direction were observed only in the salt-stressed hypothalamo-neurohypophysial neuron. The HRP-positive tubules very likely are affiliated with the lysosomal system.
利用超微结构研究了小鼠脑内多种不同类型神经元轴突和终末内质网(ER)的形态学及细胞化学特性。神经垂体受到特别关注,因为下丘脑 - 神经垂体轴突许多终末前膨体的形态和酶细胞化学活性会因慢性盐应激而改变。采用膜反差和酶细胞化学染色技术来表征轴突内质网,并确定轴突中代表溶酶体系统的细胞器以及参与天然辣根过氧化物酶(HRP)顺行轴突运输的管状结构是否与内质网相关。轴突内质网的潜在酶细胞化学标记物包括葡萄糖 - 6 - 磷酸酶(G6Pase)、硫胺焦磷酸酶、核苷二磷酸酶和酸性羟化酶活性。在未受损的下丘脑 - 神经垂体神经元以及在侧脑室接受该蛋白的小鼠的面神经和舌下运动神经元中分析了HRP的顺行运输。内质网贯穿轴突,呈现为平行的、宽20 - 40纳米的小管,通过斜向吻合相互连接。轴突内质网的膜厚度为60 - 100埃,与核周内质网相似。在正常情况下,与内质网或溶酶体相关的酶细胞化学活性在轴突和终末中不明显,但在一些轴突和终末前膨体中变得显著,这些膨体在盐应激小鼠的神经垂体中呈现出自噬样外观。在这些轴突和终末前膨体中,只有G6Pase活性是内质网的标记物。在未孵育切片和盐应激神经垂体的G6Pase细胞化学制剂中,许多内质网结构包裹或散布在分泌颗粒、多层小体和液泡周围,这些液泡可能代表参与自噬和分泌自噬的溶酶体形式。酸性水解酶活性定位于液泡以及垂体柄轴突中宽80 - 130纳米、钝端的小管内;类似的反应性小管与神经分泌细胞体中的大型次级溶酶体汇合,可能源自这些溶酶体。仅在盐应激的下丘脑 - 神经垂体神经元中观察到沿顺行方向运输HRP的形态相同的小管。HRP阳性小管很可能与溶酶体系统相关。